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Loperamide Hydrochloride Related Vomiting

Official FDA Reports1,241
Social Media Events4
Active Ingredients
  • Loperamide Hydrochloride
Additional Terms for Vomiting
  • Nausea And Vomiting
  • Throwing Up
  • N/v
  • Being Sick
  • Projectile Vomiting
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  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Imodium.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride

Imodium

Side Effects: Severe cramping and constipation. Reduced dosage from 2 pills to 1 pill to 1/2 pill. Ended up in the ER for dehydration and constipated after 4 days. Was vomiting even water.

...


Source:" IMODIUM: Side effects, ratings, and pa...

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Did the author experience vomiting while taking imodium?

What is this?

Imodium

Side Effects: Taken only once, I had severe cramping, pain, vomiting and bloating, which necessitated a trip to the ER where they thought I had appendicitis. Only after a white count and xray reveale...


Source:" viewrating.asp

View full report on drug related vomiting

Did the author experience vomiting while taking imodium?

What is this?

Imodium

I am on week 3 of Tecfedera, was having only occasional flushing, on the beginning of week 3 I had nausea and vomiting , next day diarrhea. Took Imodium and that helped. had stomach cramps for two mor...


Source:" LivingWithMultipleSclerosisHealthline/...

View full report on drug related vomiting

Did the author experience vomiting while taking imodium?

What is this?

Tell us about your Experience with Loperamide Hydrochloride Related Vomiting

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Constipation, Vomiting, Dehydration, Muscle spasms

Posted By Anonymous in askapatient.com on May 30, 2008 @ 12:00 am

Side Effects: Severe cramping and constipation. Reduced dosage from 2 pills to 1 pill to 1/2 pill. Ended up in the ER for dehydration and constipated after 4 days. Was vomiting even water. ...

Druginformer Identified Side Effects: Flatulence, Pain, Vomiting, Appendicitis, Abdominal distension, Muscle spasms

Posted By Anonymous in askapatient.com on May 19, 2007 @ 12:00 am

... cramping, pain, vomiting and bloating, which necessitated a trip to the ER where they thought I had appendicitis. Only after a white count and xray revealed I had a colon full of gas, did they cancel ...

Druginformer Identified Side Effects: Flushing, Vomiting, Abdominal pain upper

Posted By 1560213874 in facebook.com on July 1, 2013 @ 12:00 am

I am on week 3 of Tecfedera, was having only occasional flushing, on the beginning of week 3 I had nausea and vomiting, next day diarrhea. Took Imodium and that helped. had stomach cramps for two mor...

Druginformer Identified Side Effects: Vomiting

Posted By justagirl31 in healingwell.com on February 4, 2010 @ 12:00 am

I have tried taking Imodium in the past and all it did was make me throw up. I think everyone is different, I hope it works for you...



* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.